Quidel Corporation: Medical Device Recall in 2024 - (Recall #: Z-1086-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.
Product Description:

The Sofia 2 Flu + SARS Antigen FIA employs immunofluorescence technology in a sandwich design that is used with Sofia 2 to detect nucleocapsid protein from influenza A, influenza B, and SARS-CoV-2. This test allows for the detection of SARS-CoV and SARS-CoV-2, but does not differentiate between the two viruses.

Product Classification:

Class II

Date Initiated: January 3, 2024
Date Posted: February 21, 2024
Recall Number: Z-1086-2024
Event ID: 93799
Reason for Recall:

One lot of the Sofia 2 Flu + SARS Antigen FIA (Lot 709083) was labelled with incorrect expiration dates. The kits contain pouched cassettes labeled with an expiration date of May 31, 2025, however the correct expiration date for the pouches is September 12, 2024. The kits are labeled with an expiration date of April 30, 2025, however, the correct expiration date for the kits is September 12, 2024. The issue was discovered on November 28, 2023 by a supply chain employee who determined that the kits had expiration dates beyond the FDA authorized shelf life.

Status: Ongoing
Product Quantity: 312 Kits
Code Information:

UDI-DI: 30014613339229. Lot: 709083

Distribution Pattern:

US Nationwide distribution in the states of FL, TN, IL, LA, NY, IN.

Voluntary or Mandated:

Voluntary: Firm initiated